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A Hydroxypropyl Methylcellulose-Based Solid Dispersion of Curcumin with Enhanced Bioavailability and Its Hepatoprotective Activityopen access

Authors
Shin, Myoung-SookYu, Jun SangLee, JaeminJi, Young SeokJoung, Hee JoungHan, Yu-MeeYoo, Hye HyunKang, Ki Sung
Issue Date
Jul-2019
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
hydroxypropyl methylcellulose; curcumin; bioavailability; hepatoprotective
Citation
Biomolecules, v.9, no.7, pp 1 - 15
Pages
15
Indexed
SCIE
SCOPUS
Journal Title
Biomolecules
Volume
9
Number
7
Start Page
1
End Page
15
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/2796
DOI
10.3390/biom9070281
ISSN
2218-273X
2218-273X
Abstract
Curcumin is a polyphenol compound derived from the rhizomes of Curcuma longa that exhibits antioxidant, anti-inflammatory, anticancer, and antimicrobial properties. However, its low solubility in aqueous solutions, low absorption following oral administration, and rapid degradation limit its use as a functional food material. In this study, a hydroxypropyl methylcellulose-based solid dispersion of curcumin (DW-CUR 20) was prepared and its bioavailability was evaluated. In addition, its therapeutic efficacy as a hepatoprotective agent was investigated using the model of tert-butyl hydroperoxide (t-BHP)-induced hepatocyte damage. The rat plasma pharmacokinetic study showed that the oral curcumin bioavailability of DW-CUR 20 significantly increased compared to that of non-formulated curcumin. DW-CUR 20 showed a concentration-dependent hepatocyte protective effect on t-BHP-induced HepG2 cells. DW-CUR 20 inhibited the release of lactate dehydrogenase and decreased apoptosis-related proteins such as Poly (ADP-ribose) polymerase, cleaved caspase-7 and cleaved caspase-8 on t-BHP-treated HepG2 cells. These findings suggest that DW-CUR 20 could be a promising formulation for enhancing the therapeutic efficiency of curcumin and for improving the safety.
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